Genetics in keratoconus: A, B, O blood groups

Molecular studies in the GJB2 gene (Cx26) among a deaf population from Bogotá, Colombia: results of a screening program.

International journal of pediatric otorhinolaryngology·2008

Congenital anomaly rate in offspring of mothers with diabetes treated with insulin lispro during pregnancy.

Diabetic medicine : a journal of the British Diabetic Association·2005

Pre-gestational maternal body mass index predicts an increased risk of congenital malformations in infants of mothers with gestational diabetes.

Diabetic medicine : a journal of the British Diabetic Association·2005

Exstrophy of the cloaca and exstrophy of the bladder: two different expressions of a primary developmental field defect.

American journal of medical genetics·2001

Pathogenetic classification of a series of 27,145 consecutive infants with congenital defects.

American journal of medical genetics·2000

Maternal and fetal factors related to abnormal amniotic fluid.

Journal of perinatology : official journal of the California Perinatal Association·2000

Ocular toxicity of systemic chemotherapy with megadoses of carmustine and mitomycin.

Annals of ophthalmology·1994

Congenital intrastromal epithelial cyst of the iris.

Annals of ophthalmology·1994

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Annals of ophthalmology·1994

The effect of gravity on the amplitude of accommodation.

Annals of ophthalmology·1994

Tuberculous choroiditis and acquired immunodeficiency syndrome.

Annals of ophthalmology·1994

Cataract extraction with lens implantation at Biloxi Veterans Affairs Medical Center: experience of ophthalmology residents.

Annals of ophthalmology·1994

Systematic overestimation using in silico-driven curation in a population database caused reevaluation of the genetic prevalence of Alport Syndrome.

Kidney international·2026

Identification of the Novel HLA-DPB1*1989:01 Allele in a Chinese Individual by Next-Generation Sequencing.

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Characterization of a Novel, Recurrent 40.6 kb α0-Thalassemia Deletion in Canadians of East Indian Descent.

International journal of laboratory hematology·2026

GIST in Turner Syndrome.

ESMO gastrointestinal oncology·2026

Bazex-Dupré-Christol Syndrome Without Basal Cell Carcinoma Associated With a Large Interstitial Duplication at Xq26.1.

Genes, chromosomes & cancer·2026

Identification of a Novel HLA-G Allele, HLA-G*01:65, Using PolyseqOne and Oxford Nanopore Sequencing.

HLA·2026

Genetics in keratoconus: A, B, O blood groups

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Molecular studies in the GJB2 gene (Cx26) among a deaf population from Bogotá, Colombia: results of a screening program.

Congenital anomaly rate in offspring of mothers with diabetes treated with insulin lispro during pregnancy.

Pre-gestational maternal body mass index predicts an increased risk of congenital malformations in infants of mothers with gestational diabetes.

Exstrophy of the cloaca and exstrophy of the bladder: two different expressions of a primary developmental field defect.

Pathogenetic classification of a series of 27,145 consecutive infants with congenital defects.

Maternal and fetal factors related to abnormal amniotic fluid.

Ocular toxicity of systemic chemotherapy with megadoses of carmustine and mitomycin.

Congenital intrastromal epithelial cyst of the iris.

Diagnosis and treatment of orbital hemorrhagic lesions.

The effect of gravity on the amplitude of accommodation.

Tuberculous choroiditis and acquired immunodeficiency syndrome.

Cataract extraction with lens implantation at Biloxi Veterans Affairs Medical Center: experience of ophthalmology residents.

Systematic overestimation using in silico-driven curation in a population database caused reevaluation of the genetic prevalence of Alport Syndrome.

Identification of the Novel HLA-DPB1*1989:01 Allele in a Chinese Individual by Next-Generation Sequencing.

Characterization of a Novel, Recurrent 40.6 kb α0-Thalassemia Deletion in Canadians of East Indian Descent.

GIST in Turner Syndrome.

Bazex-Dupré-Christol Syndrome Without Basal Cell Carcinoma Associated With a Large Interstitial Duplication at Xq26.1.

Identification of a Novel HLA-G Allele, HLA-G*01:65, Using PolyseqOne and Oxford Nanopore Sequencing.

Genetics in keratoconus: A, B, O blood groups

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